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Index of reports
> Cases resulting in a serious event (88)
> Cases with Hypotension (11)
Below is the selection of adverse event reports related to Ranitidine that includes cases resulting in a serious event where reactions include hypotension.
Adverse event in 54 year old male receiving Ranitidine
Reported by a physician from United Kingdom on 2007-05-25
Patient: 54 year old male
Adverse reactions / side effects: Overdose, Hypotension, Haemodynamic Instability
Adverse event resulted in: hospitalization
Suspect drug(s):
Zocor
Administration route: Oral
Zocor
Administration route: Oral
Ramipril
Administration route: Oral
Ramipril
Administration route: Oral
Ranitidine
Administration route: Oral
Ranitidine
Administration route: Oral
Adverse event in 54 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-04-19
Patient: 54 year old male, weighing 113.0 kg (248.6 pounds)
Adverse reactions / side effects: PO2 Decreased, Vomiting, Diarrhoea, Hypotension, Anaesthetic Complication
Suspect drug(s):
Midazolam Hydrochloride
Dosage: 1 mg, once, intravenous
Start date: 2007-02-22
Propofol
Dosage: 1 df, once, intravenous
Start date: 2007-02-22
Dexamethasone TAB
Dosage: 4 mg, once, intravenous
Start date: 2007-02-22
Ketoprofen
Dosage: 100 mg, once, oral
Administration route: Oral
Indication: Premedication
Start date: 2007-02-22
End date: 2007-02-22
Oxygen (Oxygen)
Start date: 2007-02-22
Ranitidine
Dosage: 150 mg, oral
Administration route: Oral
Remifentanil (Remifentanil)
Dosage: 1 df, once, intravenous
Start date: 2007-02-22
Tramadol HCL
Dosage: 100 mg, once, intravenous
Indication: Perioperative Analgesia
Start date: 2007-02-22
End date: 2007-02-22
Other drugs received by patient: Chlorpheniramine Maleate; Felodipine; Ibuprofen; Acetaminophen; Hartman's (Ringer-Lactate Solution (Fresenius); Chlorhexidine (Chlorhexidine); Marcaine
Adverse event in 54 year old male receiving Ranitidine
Reported by a individual with unspecified qualification from United Kingdom on 2007-04-18
Patient: 54 year old male, weighing 113.0 kg (248.6 pounds)
Adverse reactions / side effects: PO2 Decreased, Vomiting, Diarrhoea, Hypotension
Suspect drug(s):
Dexamethasone
Dosage: 4 milligrams; daily; intravenous
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-22
Ketoprofen
Dosage: 100 milligrams; daily, oral
Administration route: Oral
Indication: Premedication
Start date: 2007-02-22
End date: 2007-02-22
Midazolam HCL
Dosage: 1 milligrams; daily, intravenous
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-22
Oxygen (Oxygen)
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-22
Propofol
Dosage: 1 dose form; daily; intravenous
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-22
Ranitidine
Dosage: 150 milligrams; unknown; oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Remifentanil (Remifentanil)
Dosage: 1 dose form; daily; intravenous
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-22
Tramadol HCL
Dosage: 100 milligrams; daily; intravenous
Indication: Perioperative Analgesia
Start date: 2007-02-22
End date: 2007-02-22
Other drugs received by patient: Chlorpheniramine Maleate; Felodipine; Ibuprofen; Paracetamol
Adverse event in 54 year old male receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-04-18
Patient: 54 year old male, weighing 113.0 kg (248.6 pounds)
Adverse reactions / side effects: PO2 Decreased, Vomiting, Diarrhoea, Restlessness, Hypotension
Suspect drug(s):
Ranitidine
Administration route: Oral
Indication: Premedication
Remifentanil
Start date: 2007-02-22
Dexamethasone 0.5mg TAB
Dosage: 4mg per day
Start date: 2007-02-22
Ketoprofen
Dosage: 100mg per day
Administration route: Oral
Indication: Premedication
Start date: 2007-02-22
End date: 2007-02-22
Midazolam HCL
Dosage: 1mg per day
Start date: 2007-02-22
Oxygen
Start date: 2007-02-22
Propofol
Start date: 2007-02-22
Tramadol HCL
Dosage: 100mg per day
Indication: Perioperative Analgesia
Start date: 2007-02-22
End date: 2007-02-22
Other drugs received by patient: Chlorpheniramine Maleate; Felodipine; Ibuprofen; Paracetamol
Adverse event in 54 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-04-16
Patient: 54 year old male, weighing 113.0 kg (248.6 pounds)
Adverse reactions / side effects: PO2 Decreased, Vomiting, Diarrhoea, Hypotension
Suspect drug(s):
Midazolam Hydrochloride
Dosage: 1 mg, intravenous
Start date: 2007-02-22
Dexamethasone TAB
Dosage: 4 mg, intravenous
Start date: 2007-02-22
Ketoprofen
Dosage: 100 mg, oral
Administration route: Oral
Indication: Premedication
Start date: 2007-02-22
End date: 2007-02-22
Oxygen(oxygen)
Start date: 2007-02-22
Propofol
Dosage: 1 df, intravenous
Start date: 2007-02-22
Ranitidine
Dosage: 150 mg, oral
Administration route: Oral
Remifentanil(remifentanil)
Dosage: 1 df, intravenous
Start date: 2007-02-22
Tramadol Hydrochloride(tramadol)
Dosage: 100 mg, intravenous
Indication: Perioperative Analgesia
Start date: 2007-02-22
End date: 2007-02-22
Other drugs received by patient: Chloepheniramine; Felodipine; Ibuprofen; Paracetamol (Acetaminophen / Paracetamol)
Adverse event in 54 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-04-12
Patient: 54 year old male, weighing 113.0 kg (248.6 pounds)
Adverse reactions / side effects: PO2 Decreased, Vomiting, Diarrhoea, Hypotension
Suspect drug(s):
Propofol
Indication: Anaesthesia
Start date: 2007-02-22
Dexamethasone
Indication: Anaesthesia
Start date: 2007-02-22
Ketoprofen
Administration route: Oral
Indication: Premedication
Start date: 2007-02-22
End date: 2007-02-22
Midazolam HCL
Indication: Anaesthesia
Start date: 2007-02-22
Oxygen
Indication: Anaesthesia
Start date: 2007-02-22
Ranitidine
Administration route: Oral
Indication: Premedication
Start date: 2007-02-22
Remifentanil
Indication: Anaesthesia
Start date: 2007-02-22
Tramadol HCL
Indication: Perioperative Analgesia
Start date: 2007-02-22
End date: 2007-02-22
Other drugs received by patient: Chlorpheniramine Maleate; Felodipine; Ibuprofen; Paracetamol; Marcaine
Adverse event in receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-04-10
Patient:
Adverse reactions / side effects: Overdose, Hypotension, Blood Pressure Decreased, Haemodynamic Instability
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace
Dosage: 300 mg, single
Administration route: Oral
Ranitidine
Dosage: 4500 mg, single
Administration route: Oral
Simvastatin
Dosage: 600 mg, single
Administration route: Oral
Adverse event in female receiving Ranitidine
Reported by a physician from Germany on 2007-03-15
Patient: female, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Hypotension, Suicide Attempt, Bradycardia, Sopor
Suspect drug(s):
Risperdal
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Katadolon
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Amitriptyline HCL
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Ibuhexal
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Metoprolol Succinate
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Seroquel
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Ranitidine
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Adverse event in 54 year old male receiving Ranitidine
Reported by a individual with unspecified qualification from United Kingdom on 2007-02-27
Patient: 54 year old male
Adverse reactions / side effects: Overdose, Hypotension, Fall
Adverse event resulted in: hospitalization
Suspect drug(s):
Ramipril
Dosage: 300 mg, unk, oral
Administration route: Oral
Ranitidine
Dosage: 4500 mg, unk, oral
Administration route: Oral
Simvastatin
Dosage: 600 mg, unk, oral
Administration route: Oral
Adverse event in receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-02-22
Patient:
Adverse reactions / side effects: Overdose, Hypotension, Blood Pressure Decreased, Haemodynamic Instability
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace
Dosage: 300 mg, single
Administration route: Oral
Ranitidine
Dosage: 4500 mg, single
Administration route: Oral
Simvastatin
Dosage: 600 mg, single
Administration route: Oral
Adverse event in 54 year old male receiving Ranitidine
Reported by a physician from United Kingdom on 2007-01-24
Patient: 54 year old male
Adverse reactions / side effects: Overdose, Hypotension
Adverse event resulted in: hospitalization
Suspect drug(s):
Zocor
Administration route: Oral
Ramipril
Ranitidine
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